Fig. 5.
Fig. 5. Antibodies to CD150 can inhibit TH2 polarization in an IFN-γ–dependent fashion. / CD4 T cells were stimulated with anti-CD3 under TH1 or TH2 conditions with or without the addition of anti-CD150 antibodies for 72 hours. Following a rest period of 48 hours in IL-2 (50 U/mL) cells were restimulated with anti-CD3 (1 μg/mL plate bound) and IL-2 (50 U/mL). In panels A and C, TH2 priming was performed with IL-4 and anti–IL-12; in panels B and D, TH2 priming was performed with IL-4 and anti–IFN-γ. Primary stimulation conditions are indicated (1°) on the x-axis. Concentrations of IFN-γ and IL-4 in culture supernatants were assayed by ELISA as outlined in “Materials and methods.” Bars represent the means of triplicate measurements.

Antibodies to CD150 can inhibit TH2 polarization in an IFN-γ–dependent fashion.

CD4 T cells were stimulated with anti-CD3 under TH1 or TH2 conditions with or without the addition of anti-CD150 antibodies for 72 hours. Following a rest period of 48 hours in IL-2 (50 U/mL) cells were restimulated with anti-CD3 (1 μg/mL plate bound) and IL-2 (50 U/mL). In panels A and C, TH2 priming was performed with IL-4 and anti–IL-12; in panels B and D, TH2 priming was performed with IL-4 and anti–IFN-γ. Primary stimulation conditions are indicated (1°) on the x-axis. Concentrations of IFN-γ and IL-4 in culture supernatants were assayed by ELISA as outlined in “Materials and methods.” Bars represent the means of triplicate measurements.

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